FIBERGRAFT BG Putty Bone Graft Substitute— 510(k) K170306

Substantially Equivalent

Prosidyan, Inc.

FDA 510(k) clearance K170306 for FIBERGRAFT BG Putty Bone Graft Substitute, Substantially Equivalent on 2017-05-24. Applicant: Prosidyan, Inc..

Clearance details

Applicant: Prosidyan, Inc.
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 2017-01-31
Decision date: 2017-05-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warren, NJ, US

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Adverse events under product code MQV

product code MQV

Death: 6
Injury: 435
Total: 441

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.